Molecular identification of sympatric chromosomal forms of Anopheles gambiae and further evidence of their reproductive isolation

• Published in: Insect molecular biology Vol. 6; no. 4; pp. 377 - 383
• Main Authors: Favia, G, della Torre, A, Bagayoko, M, Lanfrancotti, A, Sagnon, N'F, Touré, Y. T, Coluzzi, M
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Science Ltd 01.11.1997
• Subjects: Animals; Anopheles - genetics; Anopheles - physiology; Anopheles gambiae; Biological Evolution; Burkina Faso; chemotaxonomy; Crosses, Genetic; crossing; Culicidae; cytogenetics; DNA, Ribosomal - genetics; enzymes; Female; females; Freshwater; gene flow; Genetic Linkage; genetic variation; hybrids; identification; intergenic DNA; inversion polymorphism; Karyotyping; Mali; mitochondrial DNA; polymerase chain reaction; Polymerase Chain Reaction - methods; Polymorphism, Restriction Fragment Length; progeny; Reproduction; reproductive isolation; restriction fragment length polymorphism; ribosomal DNA; RNA, Ribosomal, 28S - genetics; savannas; Species Specificity; taxonomy; villages; X Chromosome - genetics; Mali; Burkina Faso
• ISSN: 0962-1075; 1365-2583
• DOI: 10.1046/j.1365-2583.1997.00189.x

Three chromosomal forms of Anopheles gambiae s.s., designated as Bamako, Mopti and Savanna, were studied for diagnostic PCR assays based on the analysis of the X‐linked ribosomal DNA (rDNA). The study was performed on a 1.3 kb fragment containing part of the 28S coding region and part of the intergenic spacer region. The amplified material was cut with fourteen restriction enzymes to detect Restriction Fragment Length Polymorphisms (RFLPs). The enzymes Tru9I and HhaI produced patterns of DNA bands which differentiated Mopti from Savanna and Bamako; moreover, a distinct ‘hybrid’ pattern was recognized in the F1 female progeny from the cross of Mopti with either one of the other two chromosomal forms. The diagnostic significance of the PCR‐RFLP assay was verified on 203 karyotyped females from field samples collected in two villages in Mali and one village in Burkina Faso. Agreement was observed between the chromosomal and the molecular identifications. No ‘hybrid’ molecular patterns were detected even among carriers of rare heterokaryotypes hypothetically produced by crosses between Mopti and Savanna. The results confirm previous observations indicating barriers to gene flow within An. gambiae s.s. and supporting the specific status of the taxonomic units proposed on cytogenetic ground.